Seaman W E, Wofsy D, Greenspan J S, Ledbetter J A
J Immunol. 1983 Apr;130(4):1713-8.
MRL/Mp-lpr/lpr (MRL/lpr) mice spontaneously develop an autoimmune disease characterized by anti-DNA antibodies, immune-complex glomerulonephritis, and massive proliferation of a distinct population of T cells. The proliferating T cells have the phenotype Thy-1.2+, T200+, Lyt-1+,2-,3-, but Thy-1.2 and Lyt-1 are expressed in abnormally low density. These cells appear to function as helper cells, and neonatal thymectomy prevents both lymphoproliferation and autoimmunity, which suggests that autoimmunity in MRL/lpr mice is secondary to T cell proliferation. We therefore attempted to reduce lymphoproliferation by treating MRL/lpr mice with a single injection of rat monoclonal antibody (MAb) to Thy-1.2 (30-H12, IgG2b). Mice were treated at 8 wk, before the onset of overt disease. We found that MRL/lpr mice were resistant to depletion of circulating T cells (CTC) by anti-Thy-1.2; 0.6 mg of antibody totally depleted CTC from normal mice, but had little or no effect on CTC in MRL/lpr mice. However, treatment with 6 mg of MAb against Thy-1.2 reduced CTC in MRL/lpr mice by over 70%. Moreover, this single treatment markedly reduced the proliferation of CTC over the ensuing 3 mo, despite clearance of the anti-Thy-1.2 from the circulation within 3 wk. Treated mice maintained better renal function than untreated controls, as assessed by levels of blood urea nitrogen (BUN), although anti-DNA antibodies were not significantly reduced. The effect of anti-Thy-1.2 was specific; treatment with rat MAb to the common leukocyte antigen T200 produced only a transient effect on circulating lymphocytes and did not reduce renal disease. The prolonged effects of a single injection of anti-Thy-1.2 suggest that the MAb produces a sustained alteration in immune regulation. The improvement in renal disease is in accord with evidence that autoimmune disease in MRL/lpr mice is T cell dependent. Monoclonal anti-lymphocyte antibodies may be useful in the treatment of autoimmunity.
MRL/Mp-lpr/lpr(MRL/lpr)小鼠会自发患上一种自身免疫性疾病,其特征为抗DNA抗体、免疫复合物性肾小球肾炎以及一类独特T细胞群体的大量增殖。增殖的T细胞具有Thy-1.2+、T200+、Lyt-1+、2-、3-的表型,但Thy-1.2和Lyt-1的表达密度异常低。这些细胞似乎发挥辅助性细胞的功能,新生期胸腺切除可预防淋巴细胞增殖和自身免疫,这表明MRL/lpr小鼠的自身免疫继发于T细胞增殖。因此,我们尝试通过给MRL/lpr小鼠单次注射抗Thy-1.2的大鼠单克隆抗体(MAb,30-H12,IgG2b)来减少淋巴细胞增殖。小鼠在8周龄、明显疾病发作之前接受治疗。我们发现MRL/lpr小鼠对抗Thy-1.2介导的循环T细胞(CTC)耗竭具有抗性;0.6毫克抗体可使正常小鼠的CTC完全耗竭,但对MRL/lpr小鼠的CTC几乎没有影响。然而,用6毫克抗Thy-1.2单克隆抗体治疗可使MRL/lpr小鼠的CTC减少70%以上。此外,尽管抗Thy-1.2在3周内从循环中清除,但这一单次治疗在随后3个月内显著降低了CTC的增殖。通过血尿素氮(BUN)水平评估,治疗后的小鼠肾功能维持得比未治疗的对照组更好,尽管抗DNA抗体没有显著减少。抗Thy-1.2的作用具有特异性;用大鼠抗常见白细胞抗原T200单克隆抗体治疗仅对循环淋巴细胞产生短暂影响,并未减轻肾脏疾病。单次注射抗Thy-1.2的长期效果表明该单克隆抗体在免疫调节方面产生了持续改变。肾脏疾病的改善与MRL/lpr小鼠自身免疫性疾病依赖T细胞的证据相符。单克隆抗淋巴细胞抗体可能对自身免疫性疾病的治疗有用。